Canonical Allele Identifier: CA1173064532

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259536T= , CM000663.2:g.67259536T=	GRCh38
NC_000001.10:g.67725219T= , CM000663.1:g.67725219T=	GRCh37
NC_000001.9:g.67497807T=	NCBI36
NG_011498.1:g.98051T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347310.10:c.*408T= MANE Select	ENSP00000321345.5:n.*408T=
ENST00000347310.9:c.*408T=	ENSP00000321345.5:n.*408T=
ENST00000395227.2:c.*408T=	ENSP00000378652.2:n.*408T=
ENST00000473881.2:c.*1124T=	ENSP00000486667.1:n.*1124T=
NM_144701.2:c.*408T=	NP_653302.2:n.*408T=
XM_005270516.2:c.*408T=	XP_005270573.1:n.*408T=
XM_011540789.1:c.*408T=	XP_011539091.1:n.*408T=
XM_011540790.1:c.*408T=	XP_011539092.1:n.*408T=
XM_011540791.1:c.*408T=	XP_011539093.1:n.*408T=
XM_011540790.3:c.*408T=	XP_011539092.1:n.*408T=
XM_011540791.3:c.*408T=	XP_011539093.1:n.*408T=
NM_144701.3:c.*408T= MANE Select	NP_653302.2:n.*408T=